Canonical Allele Identifier: PA2828012344
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133522

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser2337Leu
CA013717
NM_001354905.2:c.7010C>T